| Identification | More | [Name]
N-(Bromomethyl)phthalimide | [CAS]
5332-26-3 | [Synonyms]
N-(BROMOMETHYL)PHTALIMIDE
N-(BROMOMETHYL)PHTHALIMIDE
N-PHTHALIMIDOMETHYL BROMIDE
PHTHALIMIDOMETHYL BROMIDE
1H-Isoindole-1,3(2H)-dione, 2-(bromomethyl)-
2-(Bromomethyl)-1H-isoindole-1,3(2H)-dione
2-(bromomethyl)-1h-isoindole-3(2h)-dione
Phthalimide, N-(bromomethyl)-
N-(Bromomethyl)phthalimide,98+%
2-(Bromomethyl)isoindole-1,3-dione
2-(Bromomethyl)isoindoline-1,3-dione | [EINECS(EC#)]
226-239-2 | [Molecular Formula]
C9H6BrNO2 | [MDL Number]
MFCD00005897 | [Molecular Weight]
240.05 | [MOL File]
5332-26-3.mol |
| Chemical Properties | Back Directory | [Appearance]
white powder | [Melting point ]
152-155 °C(lit.)
| [Boiling point ]
318.9±25.0 °C(Predicted) | [density ]
1.6838 (rough estimate) | [refractive index ]
1.6120 (estimate) | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [form ]
Crystalline Powder | [pka]
-2.72±0.20(Predicted) | [color ]
White to off-white | [Water Solubility ]
decomposes | [Sensitive ]
Moisture & Light Sensitive | [BRN ]
140943 | [InChI]
1S/C9H6BrNO2/c10-5-11-8(12)6-3-1-2-4-7(6)9(11)13/h1-4H,5H2 | [InChIKey]
UUSLLECLCKTJQF-UHFFFAOYSA-N | [SMILES]
BrCN1C(=O)c2ccccc2C1=O | [CAS DataBase Reference]
5332-26-3(CAS DataBase Reference) | [NIST Chemistry Reference]
N-bromomethylphthalimide(5332-26-3) | [EPA Substance Registry System]
5332-26-3(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [F ]
8-10-21 | [TSCA ]
Yes | [HS Code ]
29251995 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
white powder | [Uses]
N-(Bromomethyl)phthalimide was used as initiator in synthesis of α-phthalimidopoly(styrene) by atom transfer radical polymerisation. It was also used in synthesis of functionalized 5-(aminomethyl)pyrimidine-2,4,6-trione analog and new bis-C(cage)-substituted o-carborane. |
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